Results 51 to 60 of about 273,607 (146)

Multispeciality Approach in the Management of Patient with Hereditary Gingival Fibromatosis: 1‐Year Followup: A Case Report

open access: yesInternational Journal of Dentistry, Volume 2010, Issue 1, 2010., 2010
Background. Hereditary gingival fibromatosis is a fibrotic enlargement of the gingiva. It may exist as an isolated abnormality or as part of multisystem syndrome. This paper reports a case of 16‐year‐old male with generalized severe gingival overgrowth, involving the maxillary and mandibular arches and covering almost all teeth. Methods.
T. Ramakrishnan   +2 more
wiley   +1 more source

Juvenile hyaline fibromatosis in siblings

open access: yesIndian Journal of Dermatology, Venereology and Leprology, 2005
Juvenile hyaline fibromatosis (JHF) is a rare, autosomal recessively inherited disorder. We report two siblings with multiple large tumors on the scalp, translucent papules on the nape of the neck, hypertrophic gingiva, and severe flexural contractures of large joints.
L K, Gupta   +5 more
openaire   +2 more sources

Anaesthesia and juvenile hyaline fibromatosis

open access: yesBritish Journal of Anaesthesia, 1996
Juvenile hyaline fibromatosis is a rare autosomal recessive disease characterized by large cutaneous nodules, especially around the head and neck and often involving the lips. The effects become increasingly severe with age and also include joint contractures, gingival hypertrophy and osteolytic lesions.
B, Norman, N, Soni, N, Madden
openaire   +2 more sources

Oral Juvenile Hyaline Fibromatosis: A Rare Entity [PDF]

open access: yes, 2011
Juvenilna hijalina fibomatoza iznimno je rijedak poremećaj kod dojenčadi i djece, a javlja se prema zakonima autosomno recesivnog nasljeđivanja. Izgleda poput multiple kožne ili subkutane tumorne tvorbe, sporo se razvija i češća je u području glave i ...
Kotrashetti, Vijayalakshmi S.   +5 more
core   +1 more source

Juvenile hyaline fibromatosis and infantile systemic hyalinosis: Divergent expressions of the same genetic defect? [PDF]

open access: yes, 2008
We describe here a three year-old girl with classic clinical and histological features of juvenile hyaline fibromatosis. We found a history of similar skin findings in her eldest sister, in whom the disorder took a rapidly progressive and fatal course in
Dhingra, Mandeep   +3 more
core   +2 more sources

Juvenile hyaline fibromatosis. A case report of a localized form?

open access: yes, 1994
Juvenile hyaline fibromatosis is a rare soft-tissue, tumor-like condition that usually arises in children. We report a case characterized by localized lesions and very slow progression. We postulate the existence of two distinct forms of juvenile hyaline
P. Orabona   +11 more
core   +1 more source

Caso para diagnóstico Case for diagnosis

open access: yesAnais Brasileiros de Dermatologia, 2009
Fibromatose hialina juvenil e hialinose sistêmica infantil são desordens autossômicas recessivas, raras da infância. À histologia, há depósito de material hialino na derme e subcutâneo. As características clínicas principais são: lesões pápulo-nodulares,
Flávia Vieira Brandão   +3 more
doaj   +1 more source

Fibromatosis of the Plantar Fascia: Diagnosis and Indications For Surgical Treatment [PDF]

open access: yes, 1999
Plantar fibromatosis is a rare, benign lesion involving the plantar aponeurosis. Eleven patients (13 feet) underwent 24 operations, including local excision, wide excision, or complete plantar fasciectomy. Clinical results were evaluated retrospectively.
Lienemann, Andreas   +4 more
core   +1 more source

Juvenile Hyaline Fibromatosis: A 47-Year Follow-UP

open access: yes, 1999
Approximately 40 cases of juvenile hyaline fibromatosis have been reported to date. This condition has not previously been described in the plastic surgery literature.
Imad L Kaddoura, Amjad A Mufarrij
core   +1 more source

Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome

open access: yesThe Turkish Journal of Pediatrics
Background. Hyaline fibromatosis syndrome is a rare autosomal recessive disorder caused by ANTXR2 pathogenic variants. The disorder is characterized by the deposition of amorphous hyaline material in connective tissues.
Tuğba Daşar   +6 more
doaj   +1 more source

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